BRCA1 promoter methylation in peripheral blood DNA of mutation negative familial breast cancer patients with a BRCA1tumour phenotype
- Cameron Snell†1,
- Michael Krypuy†1,
- Ee Ming Wong1, 2,
- kConFab investigators,
- Maurice B Loughrey1, 3 and
- Alexander Dobrovic1, 2Email author
© Snell et al.; licensee BioMed Central Ltd. 2008
Received: 12 November 2007
Accepted: 12 February 2008
Published: 12 February 2008
Individuals with germline mutations in the BRCA1 gene have an elevated risk of developing breast cancer, and often display characteristic clinicopathological features. We hypothesised that inactivation of BRCA1 by promoter methylation could occur as a germline or an early somatic event that predisposes to breast cancer with the phenotype normally associated with BRCA1 germline mutation.
We examined seven cases from breast-ovarian cancer families with tumours that showed BRCA1-like pathology but did not have detectable BRCA1 or BRCA2 germline mutations present. Methylation levels were tested by several quantitative techniques including MethyLight, methylation-sensitive high resolution melting (MS-HRM) and a newly developed digital MS-HRM assay.
In one patient, methylation of 10% of the BRCA1 alleles was detected in the peripheral blood DNA, consistent with 20% of cells having one methylated allele. Buccal mucosa DNA from this individual displayed approximately 5% BRCA1 methylation. In two other patients, methylation of BRCA1 was detected in the peripheral blood at significantly lower but still readily detectable levels (approximately 1%). Tumour DNAs from these three patients were heavily methylated at BRCA1. The other patients had no detectable BRCA1 methylation in their peripheral blood. One of seven age-matched controls showed extremely low levels of methylation in their peripheral blood (approximately 0.1%).
These results demonstrate that in some cases of breast cancer, low-level promoter methylation of BRCA1 occurs in normal tissues of the body and is associated with the development of BRCA1-like breast cancer.
In 1994, BRCA1 was identified as the first major gene associated with familial breast cancer predisposition . Since then many inactivating mutations in BRCA1 have been identified as breast cancer predisposition alleles.
Breast cancers associated with BRCA1 mutations often show characteristic histological features including high grade, high mitotic count, solid architecture and prominent lymphocytic infiltrates, all features resembling so-called medullary cancer [2–4]. BRCA1-associated tumours are usually negative by immunohistochemistry for the oestrogen receptor (ER), the progesterone receptor (PR) and HER2 [5–7]. However, the majority of breast cancers that exhibit a BRCA1-like phenotype do not harbour detectable germline mutations in BRCA1. Some of this discordance may be due to epigenetic defects in breast cancer susceptibility genes such as BRCA1 contributing to breast cancer predisposition.
Recent reports of somatic methylation (or epimutations) affecting an allele of the MLH1 gene in patients with hereditary non-polyposis colorectal cancer indicate inactivation of tumour suppressor genes by promoter methylation can occur early in development or possibly in the germline [8–10]. Allelic methylation is functionally equivalent to a mutation in that loss of activity of the second allele arising from a mutation, loss of heterozygosity or a second methylation event will inactivate the gene.
Methylation of the BRCA1 promoter has been shown to occur in approximately 20% of breast cancer patients [11–14]. Sporadic tumours with BRCA1 promoter methylation have been reported to be ER and PR negative [13, 14], or to display similar pathological features to those of BRCA1-mutated hereditary breast cancers . Furthermore, tumours with BRCA1 methylation appear to have similar global gene expression profiles to BRCA1 mutated tumours  and similar genomic copy number profiles .
Other authors have claimed that BRCA1 methylated tumours have distinct pathologies to those seen in BRCA1 mutated tumours . The discrepancy may at least in part be resolved by the hypothesis that the timing of BRCA1 methylation will influence tumour phenotype; the earlier in tumorigenesis methylation occurs, the greater the similarity to tumours arising from germline BRCA1 mutations. It must also be taken into consideration that while most tumours arising in BRCA1 mutation carriers have typical pathology, a sizeable minority do not.
We hypothesised that some individuals are predisposed to develop breast cancer with the features associated with BRCA1 mutations because they carry a methylated BRCA1 allele in their somatic tissues.
Materials and methods
Individuals and study samples
The research was completed in compliance with the Helsinki Declaration. The Ethics of Human Research Committee of Peter MacCallum Cancer Centre approved the study (approval number 02/70). Individuals used in the study were enrolled in the Kathleen Cuningham Consortium for Research in Familial Breast Cancer (kConFab). kConFab identified seven breast cancer cases (KCF1-7) with BRCA1-like features for analysis. kConFab provided DNA extracted from peripheral blood leukocytes from each case and DNA from buccal mucosa of patient KCF3. Tumour material from the KCF1, KCF2, KCF3, KCF4 and KCF6 cases was available. Four unstained, formalin-fixed, paraffin-embedded sections from each tumour were provided for analysis. DNA was extracted from the paraffin sections using the DNeasy tissue kit (Qiagen, Hilden, Germany). Normal control DNAs were provided by the Peter MacCallum Cancer Centre tissue bank.
CpGenome Universal Methylated DNA (Chemicon, Millipore, Billerica, MA, USA) was used as the 100% methylated control and DNA extracted from peripheral blood mononuclear cells of normal individuals was used as unmethylated control DNA. Bisulfite modification of DNA was performed with the MethylEasy kit (Human Genetic Signatures, Sydney, Australia) according to the manufacturer's instructions. Methylation standards were constructed by diluting 100% methylated control DNA (bisulfite modified) in a pool of normal DNA (bisulfite modified) at 50%, 25%, 10%, 5% and 1% ratios.
Experiments were performed on the RotorGene™ 3000 (MethyLight assays) and RotorGene™ 6000 (MS-HRM assays) instruments (Corbett Research, Sydney, Australia). The MethyLight data was analysed by obtaining the take-off (Ct) and amplification efficiency values for each sample for BRCA1 and HMBS from the comparative quantitation tab of the RotorGene™ analysis software and comparing them to the values for the 100% methylated DNA according to the Pfaffl method of relative quantification .
Digital MS-HRM was developed to confirm the results of the BRCA1 MethyLight and MS-HRM assays. Serial 10-fold dilutions of bisulfite modified DNA from the methylation positive samples were made and replicates of each dilution were amplified by MS-HRM. The dilution at which amplification of some replicates dropped out was then chosen for further analysis. Multiple replicate amplifications for the selected dilution were performed and compared to 0% and 100% methylated control DNA. Reactions or 'clones' resembling fully methylated and unmethylated DNA were then used in a second round amplification with M13 tagged primers. The products were then sequenced using M13 primers using the BigDye terminator kit (Applied Biosystems, Foster City, CA, USA).
We examined the peripheral blood leukocyte DNA of seven breast cancer cases (KCF1 to KCF7) (ages of onset ranging from 35 to 51 years) for BRCA1 methylation. Each of these cases, from the kConFab familial cancer repository, had a family history of breast or ovarian cancer with BRCA1-like breast pathology as defined by kConFab criteria, but were negative for mutations in the coding regions of BRCA1 and BRCA2.
We used both real-time methylation specific PCR (MethyLight)  and methylation-sensitive high resolution melting (MS-HRM)  to assess methylation levels. The primers for each assay spanned the proximal BRCA1 promoter region and were carefully designed so that the methylation status of the highly homologous pseudo BRCA1 region  was not assessed (Figure 1). Three of the individuals showed detectable BRCA1 methylation in DNA from their peripheral blood leukocytes, but unexpectedly all showed less than the 50% methylation that would be expected for methylation at one allele in every cell.
To verify that the deviation from the expected 50% methylation was not due to PCR bias or other artefacts, we developed a third methodology specifically to accurately quantify the levels of methylation. Digital MS-HRM is an adaptation of MS-HRM that enables rapid counting of methylated and unmethylated alleles. The digital approach to quantification has been described previously . However, previous methods have relied on subsequent secondary analysis whereas HRM uses in-tube analysis with a consequent rapid generation of results.
In digital MS-HRM, bisulfite modified DNA is diluted to the point where the individual PCR reactions contained 0, 1 or occasionally 2 amplifiable templates. This eliminates the problem of PCR bias where unmethylated or methylated templates have different amplification efficiencies, hence skewing the actual methylated to unmethylated ratios. Multiple replicates of the diluted sample are amplified by PCR where it is expected that many reactions will not amplify because of the absence of template. The melting profile of each reaction or 'clone' is then used to determine its methylation status. The proportion of methylation in a sample can be readily estimated by comparing the number of reactions with a peak with elevated melting temperature characteristic of methylation, over those with an lower melting temperature unmethylated peak.
Representative methylated and unmethylated clones from the digital MS-HRM experiments were sequenced to confirm the methylation status (Figure 3). A stretch of 22 bases containing four CpG sites was analysed. For the peripheral blood DNA of KCF3 (Figure 3), four of the six methylated clones had a cytosine present at all four CpGs, confirming the methylation seen by other methodologies. One clone had cytosines present at all CpGs sites but also had an additional cytosine present at a conversion site where a thymine would be expected, preceding a CpG site. The other non-CpG cytosines were converted indicating that this corresponded to a methylated allele. For one other clone only two of the CpGs were methylated but this may have been due to incomplete conversion.
Patient KCF3 developed two breast cancers in her lifetime, the first at 43 years and the second at 51 years. DNA from the first tumour was available for analysis and both MethyLight and MS-HRM assays indicated that BRCA1 methylation was present. Analysis using digital MS-HRM estimated the tumour methylation at 61% (14/23 clones).
We examined the peripheral blood and tumour DNA of KCF3 for methylation at other loci that are commonly methylated in breast cancer to assess whether the observed BRCA1 methylation was due to a propensity to methylate at a global level. The samples were screened with MethyLight. None of RASSF1A, RARB, GSTP1, TWIST, CDH1, HIC1 and HIN1 proved to be methylated (results not shown) indicating that the methylation in this patient seen is not part of an overall increased methylation of CpG islands.
Tumour material was available from two of the four patients that did not have any detectable levels of methylation in peripheral blood DNA. These tumours showed no BRCA1 methylation using MethyLight or MS-HRM, indicating that methylation of BRCA1 in the peripheral blood corresponds to tumour methylation.
The peripheral blood leukocyte DNA of seven age-matched normal controls was examined for BRCA1 methylation for comparison to the breast cancer patients. Six of the seven control samples did not have any detectable BRCA1 methylation by MethyLight or MS-HRM. One sample produced a methylated signal for two of three replicates by MethyLight only, estimated at the level of 0.1% relative to the 100% methylated control.
It is pertinent to consider the region that was spanned by the primers in each of our assays (Figure 1). In all cases, we designed primers that would not amplify the highly homologous duplication of the BRCA1 promoter region and exons 1 and 2 . The MS-HRM assay overlaid the proximal promoter region and assessed the CpGs at -37, -29, -21 and -19 according to the nomenclature of Rice et al. . Previous authors have shown some methylation in this region, commonly at -37 and -29 in peripheral blood in individuals with and without breast cancer [24, 25]. We observed methylation in only three individuals using both MS-HRM and MethyLight assays. The MethyLight assay, while overlapping this region (the 3' ends of each primer being at -37 and +27), would only give a positive result if there were methylation at the probe binding site covering CpGs at +14, +16 and +19. This indicates that the three peripheral blood DNAs with detectable methylation were all methylated over a wider region than just -37 and -29. Remarkably, all three patients had tumours that were methylated for BRCA1 as measured by both assays. The -37 and -29 CpG sites could possibly represent a seeding area where under conditions of epigenetic instability, methylation of this small region would spread to the entire promoter causing inactivation of the entire BRCA1 promoter region.
Detailed analysis of the digital HRM assay was also instructive. Whereas the region assessed included -37 and -29, it also included the CpGs at -21 and -19 that tend not to be methylated. When the individual sequences of the amplified alleles were examined, all but one showed methylation at all four sites.
In this study, we demonstrate the presence of BRCA1 promoter methylation in normal non-epithelial tissues of patients that developed breast cancer. The levels of BRCA1 methylation in the peripheral blood (and buccal mucosa for KCF3) were confirmed by three independent methods, MethyLight, MS-HRM and digital MS-HRM. The observed methylation is not due to disseminated breast cancer cells in the blood because these do not occur at sufficiently high levels to be detected by our assay. Chen et al. have also looked for BRCA1 methylation in BRCA1 and BRCA2 mutation-negative women with a family history of breast cancer . They did not detect any methylation in 41 patients. Each of these patients had approximately 10 clones examined, which would have made it difficult to detect low numbers of fully methylated alleles especially if there was any PCR bias in the amplification prior to cloning. It should also be noted that these women were unselected for BRCA1-like features and that the BRCA1 methylation status of their tumours was unknown.
We observed one peripheral blood leukocyte DNA sample in our age-matched control panel that had an extremely low level of BRCA1 methylation. This low level of methylation was not detectable by the MS-HRM assay. However, this result does raise the question of whether this individual does have an elevated risk of developing breast cancer in the future.
Many other questions remain to be addressed in future research following the intriguing findings presented here. Our results raise the possibility that methylation and associated silencing of BRCA1 could represent a germline alteration that underlies some cases of familial breast cancer. DNA from the parents of individual KCF3 were not available, so we were unable to determine if this was an epimutation that may have been inherited. In retrospect, patients from cancer families may not be the best subjects to examine for somatic methylation because of the likely limited transmissibility through the germline .
It is unclear why the levels of methylation in the somatic tissues were not at the 50% level that we expected. An interesting parallel may be drawn to a recent study showing somatic methylation in a hereditary non-polyposis colorectal cancer family. About 10% of the MSH2 gene alleles that segregated with the disease were methylated in DNA from peripheral blood . The alteration was stably inherited in numerous individuals with the disease haplotype. The inheritance was not of a methylated allele per se, but of a propensity to methylate that was presumably associated with the allelic sequence. Although a methylation propensity could explain the deviation seen from expected allelic methylation ratios in our results, upstream sequencing of KCF3 (data not shown) did not detect any possible variation that could account for this.
Our findings represent a new paradigm for somatic methylation leading to disease predisposition. Rather than an allelic methylation as has previously been reported for MLH1, a mosaic level of BRCA1 methylation has been identified in the somatic tissues of some breast cancer patients. We believe it will be important to examine individuals with early onset or multifocal breast cancer for BRCA1 methylation lacking a strong family history. We consider that widespread somatic methylation of BRCA1 is an important and as yet unrecognised cause of some BRCA1-like cancers. Further studies will be required to determine the frequency and functional significance of widespread somatic BRCA1 methylation.
Kathleen Cuningham Consortium for Research in Familial Breast Cancer
methylation-sensitive high resolution melting
We thank Melissa Brown and Stephen Fox for helpful advice and critical reading of the manuscript. Georgia Chenevix-Trench suggested that we use the kConFab resource to look for patients with germline BRCA1 methylation and Heather Thorne and Joe Sambrook who assisted with access to additional patient material.
We wish to thank Heather Thorne, Eveline Niedermayr, all the kConFab research nurses and staff, the heads and staff of the Family Cancer Clinics, and the Clinical Follow Up Study (funded by NHMRC grants 145684, 288704 and 454508) for their contributions to the kConFab resource, and the many families who contribute to kConFab. kConFab is supported by grants from the National Breast Cancer Foundation, the National Health and Medical Research Council (NHMRC) and by the Queensland Cancer Fund, the Cancer Councils of New South Wales, Victoria, Tasmania and South Australia, and the Cancer Foundation of Western Australia.
Tomasz Wojdacz designed the control MethyLight assay for HMBS. Funding for this investigation was obtained from grants to AD by the US Department of Defense, the Cancer Council of Victoria and the National Health and Medical Research Council of Australia. CS was supported by scholarships from the Peter MacCallum Cancer Centre and the Royal Australian College of Pathologists. MW was supported by the Henry and Rachel Ackman Scholarship and a studentship from The University of Melbourne.
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